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A transient conformation facilitates ligand binding to the adenine riboswitch
RNAs adopt various conformations to perform different functions in cells. Incapable of acquiring intermediates, the key initiations of ligand recognition in the adenine riboswitch have not been characterized. In this work, stopped-flow fluorescence was used to track structural switches in the full-l...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8652005/ https://www.ncbi.nlm.nih.gov/pubmed/34927032 http://dx.doi.org/10.1016/j.isci.2021.103512 |
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author | Wu, Lin Chen, Dian Ding, Jienyu Liu, Yu |
author_facet | Wu, Lin Chen, Dian Ding, Jienyu Liu, Yu |
author_sort | Wu, Lin |
collection | PubMed |
description | RNAs adopt various conformations to perform different functions in cells. Incapable of acquiring intermediates, the key initiations of ligand recognition in the adenine riboswitch have not been characterized. In this work, stopped-flow fluorescence was used to track structural switches in the full-length adenine riboswitch in real time. We used PLOR (position-selective labeling of RNA) to incorporate fluorophores into desired positions in the RNA. The switching sequence P1 responded to adenine more rapidly than helix P4 and the binding pocket, followed by stabilization of the binding pocket, P4, and annealing of P1. Moreover, a transient intermediate consisting of an unwound P1 was detected during adenine binding. These events were observed in both the WT riboswitch and a functional mutant. The findings provide insight into the conformational changes of the riboswitch RNA triggered by a ligand. |
format | Online Article Text |
id | pubmed-8652005 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-86520052021-12-17 A transient conformation facilitates ligand binding to the adenine riboswitch Wu, Lin Chen, Dian Ding, Jienyu Liu, Yu iScience Article RNAs adopt various conformations to perform different functions in cells. Incapable of acquiring intermediates, the key initiations of ligand recognition in the adenine riboswitch have not been characterized. In this work, stopped-flow fluorescence was used to track structural switches in the full-length adenine riboswitch in real time. We used PLOR (position-selective labeling of RNA) to incorporate fluorophores into desired positions in the RNA. The switching sequence P1 responded to adenine more rapidly than helix P4 and the binding pocket, followed by stabilization of the binding pocket, P4, and annealing of P1. Moreover, a transient intermediate consisting of an unwound P1 was detected during adenine binding. These events were observed in both the WT riboswitch and a functional mutant. The findings provide insight into the conformational changes of the riboswitch RNA triggered by a ligand. Elsevier 2021-11-25 /pmc/articles/PMC8652005/ /pubmed/34927032 http://dx.doi.org/10.1016/j.isci.2021.103512 Text en © 2021. https://creativecommons.org/licenses/by-nc-nd/3.0/igo/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/3.0/igo/). |
spellingShingle | Article Wu, Lin Chen, Dian Ding, Jienyu Liu, Yu A transient conformation facilitates ligand binding to the adenine riboswitch |
title | A transient conformation facilitates ligand binding to the adenine riboswitch |
title_full | A transient conformation facilitates ligand binding to the adenine riboswitch |
title_fullStr | A transient conformation facilitates ligand binding to the adenine riboswitch |
title_full_unstemmed | A transient conformation facilitates ligand binding to the adenine riboswitch |
title_short | A transient conformation facilitates ligand binding to the adenine riboswitch |
title_sort | transient conformation facilitates ligand binding to the adenine riboswitch |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8652005/ https://www.ncbi.nlm.nih.gov/pubmed/34927032 http://dx.doi.org/10.1016/j.isci.2021.103512 |
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